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Journal Abstract Search

174 related items for PubMed ID: 9605581

  • 1. [3H]-SCH 58261 labelling of functional A2A adenosine receptors in human neutrophil membranes.
    Varani K, Gessi S, Dionisotti S, Ongini E, Borea PA.
    Br J Pharmacol; 1998 Apr; 123(8):1723-31. PubMed ID: 9605581
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  • 2. Characterization of A2A adenosine receptors in human lymphocyte membranes by [3H]-SCH 58261 binding.
    Varani K, Gessi S, Dalpiaz A, Ongini E, Borea PA.
    Br J Pharmacol; 1997 Sep; 122(2):386-92. PubMed ID: 9313951
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  • 5. The non-xanthine heterocyclic compound SCH 58261 is a new potent and selective A2a adenosine receptor antagonist.
    Zocchi C, Ongini E, Conti A, Monopoli A, Negretti A, Baraldi PG, Dionisotti S.
    J Pharmacol Exp Ther; 1996 Feb; 276(2):398-404. PubMed ID: 8632302
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  • 6. [(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors.
    Varani K, Merighi S, Gessi S, Klotz KN, Leung E, Baraldi PG, Cacciari B, Romagnoli R, Spalluto G, Borea PA.
    Mol Pharmacol; 2000 May; 57(5):968-75. PubMed ID: 10779381
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  • 8. Differences in the order of potency for agonists but not antagonists at human and rat adenosine A2A receptors.
    Kull B, Arslan G, Nilsson C, Owman C, Lorenzen A, Schwabe U, Fredholm BB.
    Biochem Pharmacol; 1999 Jan 01; 57(1):65-75. PubMed ID: 9920286
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  • 10. ZM241385 is an antagonist of the facilitatory responses produced by the A2A adenosine receptor agonists CGS21680 and HENECA in the rat hippocampus.
    Cunha RA, Constantino MD, Ribeiro JA.
    Br J Pharmacol; 1997 Dec 01; 122(7):1279-84. PubMed ID: 9421273
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  • 11. Design, synthesis, and biological evaluation of a second generation of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as potent and selective A2A adenosine receptor antagonists.
    Baraldi PG, Cacciari B, Spalluto G, Bergonzoni M, Dionisotti S, Ongini E, Varani K, Borea PA.
    J Med Chem; 1998 Jun 04; 41(12):2126-33. PubMed ID: 9622554
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  • 12. Kinetic and functional properties of [3H]ZM241385, a high affinity antagonist for adenosine A2A receptors.
    Uustare A, Vonk A, Terasmaa A, Fuxe K, Rinken A.
    Life Sci; 2005 Feb 11; 76(13):1513-26. PubMed ID: 15680315
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  • 13. Effect of low frequency electromagnetic fields on A2A adenosine receptors in human neutrophils.
    Varani K, Gessi S, Merighi S, Iannotta V, Cattabriga E, Spisani S, Cadossi R, Borea PA.
    Br J Pharmacol; 2002 May 11; 136(1):57-66. PubMed ID: 11976268
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  • 14. Pharmacological and biochemical characterization of adenosine receptors in the human malignant melanoma A375 cell line.
    Merighi S, Varani K, Gessi S, Cattabriga E, Iannotta V, Ulouglu C, Leung E, Borea PA.
    Br J Pharmacol; 2001 Nov 11; 134(6):1215-26. PubMed ID: 11704641
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  • 15. Binding of [3H]KF17837S, a selective adenosine A2 receptor antagonist, to rat brain membranes.
    Nonaka H, Mori A, Ichimura M, Shindou T, Yanagawa K, Shimada J, Kase H.
    Mol Pharmacol; 1994 Nov 11; 46(5):817-22. PubMed ID: 7969067
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  • 16. Adenosine A2A receptor agonists inhibit lipopolysaccharide-induced production of tumor necrosis factor-alpha by equine monocytes.
    Sun WC, Moore JN, Hurley DJ, Vandenplas ML, Linden J, Cao Z, Murray TF.
    Vet Immunol Immunopathol; 2008 Jan 15; 121(1-2):91-100. PubMed ID: 17913243
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  • 17. Pharmacological and biochemical characterization of purified A2a adenosine receptors in human platelet membranes by [3H]-CGS 21680 binding.
    Varani K, Gessi S, Dalpiaz A, Borea PA.
    Br J Pharmacol; 1996 Apr 15; 117(8):1693-701. PubMed ID: 8732278
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  • 20. Motor stimulant effects of the adenosine A2A receptor antagonist SCH 58261 do not develop tolerance after repeated treatments in 6-hydroxydopamine-lesioned rats.
    Pinna A, Fenu S, Morelli M.
    Synapse; 2001 Mar 01; 39(3):233-8. PubMed ID: 11284438
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